Canonical Allele Identifier: CA1759352534

Gene: CSMD1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.4427963_4427964delinsAC , CM000670.2:g.4427963_4427964delinsAC	GRCh38
NC_000008.10:g.4285485_4285486delinsAC , CM000670.1:g.4285485_4285486delinsAC	GRCh37
NC_000008.9:g.4272893_4272894delinsAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000635120.2:c.303-7899_303-7898delinsGT MANE Select	ENSP00000489225.1:n.303-7899_303-7898delinsGT
ENST00000400186.7:c.303-7899_303-7898delinsGT	ENSP00000383047.3:n.303-7899_303-7898delinsGT
ENST00000520002.5:c.303-7899_303-7898delinsGT	ENSP00000430733.1:n.303-7899_303-7898delinsGT
ENST00000602557.5:c.303-7899_303-7898delinsGT	ENSP00000473359.1:n.303-7899_303-7898delinsGT
ENST00000602723.5:c.303-7899_303-7898delinsGT	ENSP00000473617.1:n.303-7899_303-7898delinsGT
ENST00000635120.1:c.303-7899_303-7898delinsGT	ENSP00000489225.1:n.303-7899_303-7898delinsGT
NM_033225.5:c.303-7899_303-7898delinsGT	NP_150094.5:n.303-7899_303-7898delinsGT
XM_011534752.1:c.303-7899_303-7898delinsGT	XP_011533054.1:n.303-7899_303-7898delinsGT
XM_011534752.2:c.303-7899_303-7898delinsGT	XP_011533054.1:n.303-7899_303-7898delinsGT
XM_017013731.1:c.303-7899_303-7898delinsGT	XP_016869220.1:n.303-7899_303-7898delinsGT
NM_033225.6:c.303-7899_303-7898delinsGT MANE Select	NP_150094.5:n.303-7899_303-7898delinsGT